Canonical Allele Identifier: CA1694876933

Gene: NPY

Linked Data

• dbSNP Id: rs1787568798

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290760_24290761insTTAAATAATA , CM000669.2:g.24290760_24290761insTTAAATAATA	GRCh38
NC_000007.13:g.24330379_24330380insTTAAATAATA , CM000669.1:g.24330379_24330380insTTAAATAATA	GRCh37
NC_000007.12:g.24296904_24296905insTTAAATAATA	NCBI36
NG_016148.1:g.11573_11574insTTAAATAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-903_270-902insTTAAATAATA MANE Select	ENSP00000242152.2:n.270-903_270-902insTTAAATAATA
ENST00000242152.6:c.270-903_270-902insTTAAATAATA	ENSP00000242152.2:n.270-903_270-902insTTAAATAATA
ENST00000405982.1:c.270-903_270-902insTTAAATAATA	ENSP00000385282.1:n.270-903_270-902insTTAAATAATA
ENST00000407573.5:c.270-903_270-902insTTAAATAATA	ENSP00000384364.1:n.270-903_270-902insTTAAATAATA
NM_000905.3:c.270-903_270-902insTTAAATAATA	NP_000896.1:n.270-903_270-902insTTAAATAATA
XM_017012910.1:c.41+28597_41+28598insATTATTTAAT	XP_016868399.1:n.41+28597_41+28598insATTATTTAAT
XM_017012911.1:c.41+28597_41+28598insATTATTTAAT	XP_016868400.1:n.41+28597_41+28598insATTATTTAAT
XR_001745121.1:n.473+28597_473+28598insATTATTTAAT
XR_001745122.1:n.345-93731_345-93730insATTATTTAAT
XR_001745123.1:n.473+28597_473+28598insATTATTTAAT
XR_001745124.1:n.473+28597_473+28598insATTATTTAAT
XR_001745125.1:n.473+28597_473+28598insATTATTTAAT
XR_001745126.1:n.473+28597_473+28598insATTATTTAAT
XR_001745127.1:n.345-35061_345-35060insATTATTTAAT
XR_001745129.1:n.473+28597_473+28598insATTATTTAAT
XR_001745130.1:n.473+28597_473+28598insATTATTTAAT
XR_001745131.1:n.473+28597_473+28598insATTATTTAAT
XR_001745132.1:n.473+28597_473+28598insATTATTTAAT
NM_000905.4:c.270-903_270-902insTTAAATAATA MANE Select	NP_000896.1:n.270-903_270-902insTTAAATAATA